Evidence map›Paper›PMID 42872197›Full record

ArticleRSC advances2026

Amphipathic peptoid transporters for protein and nanoparticle delivery.

Juhye Shin, Eun-Ji Kim, Minjae Jun, Min Uk Yang, Kok Jia Yi Erica, Jae Young Lee, Jiwon Seo, Jiyoun Lee

Abstract read
In one paragraph

Article in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Juhye ShinDepartment of Chemistry, Gwangju Institute of Science and Technology Gwangju 61005 Republic of Korea jseo@gist.ac.kr.
Eun-Ji KimDepartment of Next-Generation Applied Sciences, School of Biopharmaceutical and Medical Sciences, Sungshin Women's University Seoul 01133 Republic of Korea jlee@sungshin.ac.kr.
Minjae JunDepartment of Chemistry, Gwangju Institute of Science and Technology Gwangju 61005 Republic of Korea jseo@gist.ac.kr.
Min Uk YangDepartment of Chemistry, Gwangju Institute of Science and Technology Gwangju 61005 Republic of Korea jseo@gist.ac.kr.
Kok Jia Yi EricaSchool of Materials Science and Engineering, Gwangju Institute of Science and Technology Gwangju 61005 Republic of Korea.
Jae Young LeeSchool of Materials Science and Engineering, Gwangju Institute of Science and Technology Gwangju 61005 Republic of Korea.ORCID https://orcid.org/0000-0002-9392-5576
Jiwon SeoDepartment of Chemistry, Gwangju Institute of Science and Technology Gwangju 61005 Republic of Korea jseo@gist.ac.kr.ORCID https://orcid.org/0000-0002-5433-5071
Jiyoun LeeDepartment of Next-Generation Applied Sciences, School of Biopharmaceutical and Medical Sciences, Sungshin Women's University Seoul 01133 Republic of Korea jlee@sungshin.ac.kr.ORCID https://orcid.org/0000-0003-3819-5889

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of efficient intracellular delivery vectors requires a precise balance between cellular uptake and minimal cytotoxicity. Here, we describe a series of cationic amphipathic peptoids designed to evaluate how sequence variation controls cell penetration and uptake. The peptoid series showed substantially higher cellular uptake than previously developed peptoid transporters, while subcellular localization varied across the series. Intracellular distribution was influenced by the type and positioning of hydrophobic residues relative to guanidinium-bearing

Identifiers

PMID42872197
PMCPMC13660515

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.